[Pretreatment with dexmedetomidine ameliorates renal inflammation and oxidative stress in rats with lipopolysaccharide-induced sepsis and acute kidney injury]

Nan Fang Yi Ke Da Xue Xue Bao. 2015 Oct;35(10):1472-5.
[Article in Chinese]

Abstract

Objective: To investigate the effects of dexmedetomidine on inflammatory reaction, oxidative stress, and renal pathologies in a rat model of lipopolysaccharide (LPS)-induced sepsis.

Methods: Thirty-two SD rats were randomly divided into 4 groups, including a sham-operated group, LPS group with LPS (5 mg/kg) injection via the caudal vein 30 min before the operation, dexmedetomidine (Dex) +LPS group with additional Dex (10 µg/kg) injection via the caudal vein 10 min before LPS injection, and yohimbine+DEX+LPS group with intraperitoneal yohimbine (1 mg/kg) injection 40 min before and Dex injection 10 min before LPS injection. The levels of IL-1β, SOD and MDA in the plasma and renal tissues were determined, and the renal pathologies were examined.

Results: Compared with the sham-operated rats, the rats in LPS group showed significantly increased IL-1β and MDA levels and lowered SOD activity in the plasma and renal tissues (P<0.05) with obvious renal pathologies. Dex pretreatment obviously lowered IL-1β and MDA levels and enhanced SOD activity in the plasma and renal tissues in LPS-challenged rats (P<0.05), and significantly lessened LPS-induced renal pathologies.

Conclusion: Dex can protect the rats against LPS-induced renal injury by alleviating the inflammatory reactions and cytokine oxidative stress, and this effect is mediated possibly by α2 receptors.

MeSH terms

  • Acute Kidney Injury / drug therapy*
  • Animals
  • Dexmedetomidine / pharmacology*
  • Inflammation / drug therapy*
  • Interleukin-1beta / metabolism
  • Kidney / drug effects
  • Kidney / physiopathology
  • Lipopolysaccharides
  • Malondialdehyde / metabolism
  • Oxidative Stress*
  • Rats
  • Rats, Sprague-Dawley
  • Sepsis / chemically induced
  • Sepsis / drug therapy*
  • Superoxide Dismutase / metabolism

Substances

  • Interleukin-1beta
  • Lipopolysaccharides
  • Malondialdehyde
  • Dexmedetomidine
  • Superoxide Dismutase